TY - JOUR
T1 - The IMI PROTECT project
T2 - purpose, organizational structure, and procedures
AU - Reynolds, Robert F
AU - Kurz, Xavier
AU - de Groot, Mark C H
AU - Schlienger, Raymond G
AU - Grimaldi-Bensouda, Lamiae
AU - Tcherny-Lessenot, Stephanie
AU - Klungel, Olaf H
N1 - Copyright © 2016 John Wiley & Sons, Ltd.
PY - 2016
Y1 - 2016
N2 - The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European ConsorTium (PROTECT) initiative was a collaborative European project that sought to address limitations of current methods in the field of pharmacoepidemiology and pharmacovigilance. Initiated in 2009 and ending in 2015, PROTECT was part of the Innovative Medicines Initiative, a joint undertaking by the European Union and pharmaceutical industry. Thirty-five partners including academics, regulators, small and medium enterprises, and European Federation of Pharmaceuticals Industries and Associations companies contributed to PROTECT. Two work packages within PROTECT implemented research examining the extent to which differences in the study design, methodology, and choice of data source can contribute to producing discrepant results from observational studies on drug safety. To evaluate the effect of these differences, the project applied different designs and analytic methodology for six drug-adverse event pairs across several electronic healthcare databases and registries. This papers introduces the organizational structure and procedures of PROTECT, including how drug-adverse event and data sources were selected, study design and analyses documents were developed, and results managed centrally. Copyright © 2016 John Wiley & Sons, Ltd.
AB - The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European ConsorTium (PROTECT) initiative was a collaborative European project that sought to address limitations of current methods in the field of pharmacoepidemiology and pharmacovigilance. Initiated in 2009 and ending in 2015, PROTECT was part of the Innovative Medicines Initiative, a joint undertaking by the European Union and pharmaceutical industry. Thirty-five partners including academics, regulators, small and medium enterprises, and European Federation of Pharmaceuticals Industries and Associations companies contributed to PROTECT. Two work packages within PROTECT implemented research examining the extent to which differences in the study design, methodology, and choice of data source can contribute to producing discrepant results from observational studies on drug safety. To evaluate the effect of these differences, the project applied different designs and analytic methodology for six drug-adverse event pairs across several electronic healthcare databases and registries. This papers introduces the organizational structure and procedures of PROTECT, including how drug-adverse event and data sources were selected, study design and analyses documents were developed, and results managed centrally. Copyright © 2016 John Wiley & Sons, Ltd.
KW - pharmacoepidemiology
KW - Innovative Medicines Initiative
KW - PROTECT
KW - observational studies
KW - methodology
KW - electronic healthcare databases
KW - European Medicines Agency
U2 - 10.1002/pds.3933
DO - 10.1002/pds.3933
M3 - Article
C2 - 27038353
SN - 1053-8569
VL - 25 Suppl 1
SP - 5
EP - 10
JO - Pharmacoepidemiology and Drug Safety
JF - Pharmacoepidemiology and Drug Safety
ER -